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1977 1
1978 2
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Kappa-type light chain crystal storage histiocytosis.
Terashima K, Takahashi K, Kojima M, Imai Y, Tsuchida S, Migita S, Ebina S, Itoh C. Terashima K, et al. Acta Pathol Jpn. 1978 Jan;28(1):111-38. doi: 10.1111/j.1440-1827.1978.tb01254.x. Acta Pathol Jpn. 1978. PMID: 416650
An autopsy case of systemic histiocytosis with excessive deposition of kappa-type light chain crystals was reported in a 58 year-old man who had consistently showed kappa-type light chain paraproteinemia, Bence Jones proteinuria and hypogammaglobulinemia for …
An autopsy case of systemic histiocytosis with excessive deposition of kappa-type light chain crystals was reported in a 58 year-old man who …
Scleromyxedema myopathy. Histochemical and electron microscopic observations.
Verity MA, Toop J, McAdam LP, Pearson CM. Verity MA, et al. Am J Clin Pathol. 1978 Apr;69(4):446-51. doi: 10.1093/ajcp/69.4.446. Am J Clin Pathol. 1978. PMID: 645644
A biopsy-proven case of scleromyxedema (papular mucinosis) with IgG lambda light chain paraproteinemia, eosinophilia and severe proximal myopathy is presented. ...
A biopsy-proven case of scleromyxedema (papular mucinosis) with IgG lambda light chain paraproteinemia, eosinophilia an …
Papular mucinosis with myopathy, arthritis, and eosinophilia. A histopathologic study.
McAdam LP, Pearson CM, Pitts WH, Sadoff L, Verity MA. McAdam LP, et al. Arthritis Rheum. 1977 May;20(4):989-96. doi: 10.1002/art.1780200412. Arthritis Rheum. 1977. PMID: 405019
A patient with biopsy-proven papular mucinosis, plus the characteristic IgG lambda light chain paraproteinemia, also developed a severe proximal myopathy, seronegative inflammatory polyarthritis, and marked eosinophilia. ...No mucin deposition was detectable …
A patient with biopsy-proven papular mucinosis, plus the characteristic IgG lambda light chain paraproteinemia, also de …